Výsledky vyhledávání - Metcalf, Ginger A

The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care System Autor Feofanova, Elena Valeryevna, Zhang, Guo-Qiang, Lhatoo, Samden, Metcalf, Ginger A, Boerwinkle, Eric, Venner, Eric

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Loss-of-function variants influence the human serum metabolome Autor Yu, Bing, Li, Alexander H., Metcalf, Ginger A., Muzny, Donna M., Morrison, Alanna C., White, Simon, Mosley, Thomas H., Gibbs, Richard A., Boerwinkle, Eric

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Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic Study Autor Feofanova, Elena V., Yu, Bing, Metcalf, Ginger A., Liu, Xiaoming, Muzny, Donna, Below, Jennifer E., Wagenknecht, Lynne E., Gibbs, Richard A., Morrison, Alanna C., Boerwinkle, Eric

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Whole genome sequence analysis of serum amino acid levels Autor Yu, Bing, de Vries, Paul S., Metcalf, Ginger A., Wang, Zhe, Feofanova, Elena V., Liu, Xiaoming, Muzny, Donna Marie, Wagenknecht, Lynne E., Gibbs, Richard A., Morrison, Alanna C., Boerwinkle, Eric

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Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study Autor de Vries, Paul S., Yu, Bing, Feofanova, Elena V., Metcalf, Ginger A., Brown, Michael R., Zeighami, Atefeh L., Liu, Xiaoming, Muzny, Donna M., Gibbs, Richard A., Boerwinkle, Eric, Morrison, Alanna C.

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The gut mycobiome of the Human Microbiome Project healthy cohort Autor Nash, Andrea K., Auchtung, Thomas A., Wong, Matthew C., Smith, Daniel P., Gesell, Jonathan R., Ross, Matthew C., Stewart, Christopher J., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Ajami, Nadim J., Petrosino, Joseph F.

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Structure and function of the healthy pre-adolescent pediatric gut microbiome Autor Hollister, Emily B., Riehle, Kevin, Luna, Ruth Ann, Weidler, Erica M., Rubio-Gonzales, Michelle, Mistretta, Toni-Ann, Raza, Sabeen, Doddapaneni, Harsha V., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Petrosino, Joseph F., Shulman, Robert J., Versalovic, James

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Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation Autor Eicher, John D., Chen, Ming-Huei, Pitsillides, Achilleas N., Lin, Honghuang, Veeraraghavan, Narayanan, Brody, Jennifer A., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Becker, Diane M., Becker, Lewis C., Faraday, Nauder, Mathias, Rasika A., Yanek, Lisa R., Boerwinkle, Eric, Cupples, L. Adrienne, Johnson, Andrew D.

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Leveraging Human Microbiome Features to Diagnose and Stratify Children with Irritable Bowel Syndrome Autor Hollister, Emily B., Oezguen, Numan, Chumpitazi, Bruno P., Luna, Ruth Ann, Weidler, Erica M., Rubio-Gonzales, Michelle, Dahdouli, Mahmoud, Cope, Julia L., Mistretta, Toni-Ann, Raza, Sabeen, Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Petrosino, Joseph F., Heitkemper, Margaret, Savidge, Tor C., Shulman, Robert J., Versalovic, James

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Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program Autor Venner, Eric, Muzny, Donna, Smith, Joshua D., Walker, Kimberly, Neben, Cynthia L., Lockwood, Christina M., Empey, Phillip E., Metcalf, Ginger A., Kachulis, Chris, Mian, Sana, Musick, Anjene, Rehm, Heidi L., Harrison, Steven, Gabriel, Stacey, Gibbs, Richard A., Nickerson, Deborah, Zhou, Alicia Y., Doheny, Kimberly, Ozenberger, Bradley, Topper, Scott E., Lennon, Niall J.

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Fully resolved assembly of Cryptosporidium parvum Autor Menon, Vipin K, Okhuysen, Pablo C, Chappell, Cynthia L, Mahmoud, Medhat, Mahmoud, Medhat, Meng, Qingchang, Doddapaneni, Harsha, Vee, Vanesa, Han, Yi, Salvi, Sejal, Bhamidipati, Sravya, Kottapalli, Kavya, Weissenberger, George, Shen, Hua, Ross, Matthew C, Hoffman, Kristi L, Cregeen, Sara Javornik, Muzny, Donna M, Metcalf, Ginger A, Gibbs, Richard A, Petrosino, Joseph F, Sedlazeck, Fritz J

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Temporal development of the gut microbiome in early childhood from the TEDDY study Autor Stewart, Christopher J., Ajami, Nadim J., O’Brien, Jacqueline L., Hutchinson, Diane S., Smith, Daniel P., Wong, Matthew C., Ross, Matthew C., Lloyd, Richard E., Doddapaneni, HarshaVardhan, Metcalf, Ginger A., Muzny, Donna, Gibbs, Richard A., Vatanen, Tommi, Huttenhower, Curtis, Xavier, Ramnik J., Rewers, Marian, Hagopian, William, Toppari, Jorma, Ziegler, Anette-G., She, Jin-Xiong, Akolkar, Beena, Lernmark, Ake, Hyoty, Heikki, Vehik, Kendra, Krischer, Jeffrey P., Petrosino, Joseph F.

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Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk Autor Yu, Bing, Pulit, Sara L., Hwang, Shih-Jen, Brody, Jennifer A., Amin, Najaf, Auer, Paul L., Bis, Joshua C., Boerwinkle, Eric, Burke, Gregory L., Chakravarti, Aravinda, Correa, Adolfo, Dreisbach, Albert W., Franco, Oscar H., Ehret, Georg B., Franceschini, Nora, Hofman, Albert, Lin, Dan-Yu, Metcalf, Ginger A., Musani, Solomon K., Muzny, Donna, Palmas, Walter, Raffel, Leslie, Reiner, Alex, Rice, Ken, Rotter, Jerome I., Veeraraghavan, Narayanan, Fox, Ervin, Guo, Xiuqing, North, Kari E., Gibbs, Richard A., van Duijn, Cornelia M., Psaty, Bruce M., Levy, Daniel, Newton-Cheh, Christopher, Morrison, Alanna C.

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Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications Autor Murdock, David R., Venner, Eric, Muzny, Donna M., Metcalf, Ginger A., Murugan, Mullai, Hadley, Trevor D., Chander, Varuna, De Vries, Paul, Jia, Xiaoming, Hussain, Aliza, Agha, Ali M., Sabo, Aniko, Li, Shoudong, Meng, Qingchang, Hu, Jianhong, Tian, Xia, Cohen, Michelle, Yi, Victoria, Kovar, Christie L., Gingras, Marie-Claude, Korchina, Viktoriya, Howard, Chad, Riconda, Daniel L., Pereira, Stacey, Smith, Hadley, Huda, Zohra A., Buentello, Alexandria, Marino, Patricia R., Leiber, Lee, Balasubramanyam, Ashok, Amos, Christopher I., Civitello, Andrew, Chelu, Mihail G., Maag, Ronald, McGuire, Amy L., Boerwinkle, Eric, Wehrens, Xander H.T., Ballantyne, Christie M., Gibbs, Richard A.

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Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts Autor Raffield, Laura M., Iyengar, Apoorva K., Wang, Biqi, Gaynor, Sheila M., Spracklen, Cassandra N., Zhong, Xue, Kowalski, Madeline H., Salimi, Shabnam, Polfus, Linda M., Benjamin, Emelia J., Bis, Joshua C., Bowler, Russell, Cade, Brian E., Choi, Won Jung, Comellas, Alejandro P., Correa, Adolfo, Cruz, Pedro, Doddapaneni, Harsha, Durda, Peter, Gogarten, Stephanie M., Jain, Deepti, Kim, Ryan W., Kral, Brian G., Lange, Leslie A., Larson, Martin G., Laurie, Cecelia, Lee, Jiwon, Lee, Seonwook, Lewis, Joshua P., Metcalf, Ginger A., Mitchell, Braxton D., Momin, Zeineen, Muzny, Donna M., Pankratz, Nathan, Park, Cheol Joo, Rich, Stephen S., Rotter, Jerome I., Ryan, Kathleen, Seo, Daekwan, Tracy, Russell P., Viaud-Martinez, Karine A., Yanek, Lisa R., Zhao, Lue Ping, Lin, Xihong, Li, Bingshan, Li, Yun, Dupuis, Josée, Reiner, Alexander P., Mohlke, Karen L., Auer, Paul L.

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Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program Autor Hu, Xiaowei, Qiao, Dandi, Kim, Wonji, Moll, Matthew, Balte, Pallavi P., Lange, Leslie A., Bartz, Traci M., Kumar, Rajesh, Li, Xingnan, Yu, Bing, Cade, Brian E., Laurie, Cecelia A., Sofer, Tamar, Ruczinski, Ingo, Nickerson, Deborah A., Muzny, Donna M., Metcalf, Ginger A., Doddapaneni, Harshavardhan, Gabriel, Stacy, Gupta, Namrata, Dugan-Perez, Shannon, Cupples, L. Adrienne, Loehr, Laura R., Jain, Deepti, Rotter, Jerome I., Wilson, James G., Psaty, Bruce M., Fornage, Myriam, Morrison, Alanna C., Vasan, Ramachandran S., Washko, George, Rich, Stephen S., O’Connor, George T., Bleecker, Eugene, Kaplan, Robert C., Kalhan, Ravi, Redline, Susan, Gharib, Sina A., Meyers, Deborah, Ortega, Victor, Dupuis, Josée, London, Stephanie J., Lappalainen, Tuuli, Oelsner, Elizabeth C., Silverman, Edwin K., Barr, R. Graham, Thornton, Timothy A., Wheeler, Heather E., Cho, Michael H., Im, Hae Kyung, Manichaikul, Ani

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Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants Autor Zhao, Xutong, Qiao, Dandi, Yang, Chaojie, Kasela, Silva, Kim, Wonji, Ma, Yanlin, Shrine, Nick, Batini, Chiara, Sofer, Tamar, Taliun, Sarah A. Gagliano, Sakornsakolpat, Phuwanat, Balte, Pallavi P., Prokopenko, Dmitry, Yu, Bing, Lange, Leslie A., Dupuis, Josée, Cade, Brian E., Lee, Jiwon, Gharib, Sina A., Daya, Michelle, Laurie, Cecelia A., Ruczinski, Ingo, Cupples, L. Adrienne, Loehr, Laura R., Bartz, Traci M., Morrison, Alanna C., Psaty, Bruce M., Vasan, Ramachandran S., Wilson, James G., Taylor, Kent D., Durda, Peter, Johnson, W. Craig, Cornell, Elaine, Guo, Xiuqing, Liu, Yongmei, Tracy, Russell P., Ardlie, Kristin G., Aguet, François, VanDenBerg, David J., Papanicolaou, George J., Rotter, Jerome I., Barnes, Kathleen C., Jain, Deepti, Nickerson, Deborah A., Muzny, Donna M., Metcalf, Ginger A., Doddapaneni, Harshavardhan, Dugan-Perez, Shannon, Gupta, Namrata, Gabriel, Stacey, Rich, Stephen S., O’Connor, George T., Redline, Susan, Reed, Robert M., Laurie, Cathy C., Daviglus, Martha L., Preudhomme, Liana K., Burkart, Kristin M., Kaplan, Robert C., Wain, Louise V., Tobin, Martin D., London, Stephanie J., Lappalainen, Tuuli, Oelsner, Elizabeth C., Abecasis, Goncalo R., Silverman, Edwin K., Barr, R. Graham, Cho, Michael H., Manichaikul, Ani

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Somatic mutations affect key pathways in lung adenocarcinoma Autor Ding, Li, Getz, Gad, Wheeler, David A., Mardis, Elaine R., McLellan, Michael D., Cibulskis, Kristian, Sougnez, Carrie, Greulich, Heidi, Muzny, Donna M., Morgan, Margaret B., Fulton, Lucinda, Fulton, Robert S., Zhang, Qunyuan, Wendl, Michael C., Lawrence, Michael S., Larson, David E., Chen, Ken, Dooling, David J., Sabo, Aniko, Hawes, Alicia C., Shen, Hua, Jhangiani, Shalini N., Lewis, Lora R., Hall, Otis, Zhu, Yiming, Mathew, Tittu, Ren, Yanru, Yao, Jiqiang, Scherer, Steven E., Clerc, Kerstin, Metcalf, Ginger A., Ng, Brian, Milosavljevic, Aleksandar, Gonzalez-Garay, Manuel L., Osborne, John R., Meyer, Rick, Shi, Xiaoqi, Tang, Yuzhu, Koboldt, Daniel C., Lin, Ling, Abbott, Rachel, Miner, Tracie L., Pohl, Craig, Fewell, Ginger, Haipek, Carrie, Schmidt, Heather, Dunford-Shore, Brian H., Kraja, Aldi, Crosby, Seth D., Sawyer, Christopher S., Vickery, Tammi, Sander, Sacha, Robinson, Jody, Winckler, Wendy, Baldwin, Jennifer, Chirieac, Lucian R., Dutt, Amit, Fennell, Tim, Hanna, Megan, Johnson, Bruce E., Onofrio, Robert C., Thomas, Roman K., Tonon, Giovanni, Weir, Barbara A., Zhao, Xiaojun, Ziaugra, Liuda, Zody, Michael C., Giordano, Thomas, Orringer, Mark B., Roth, Jack A., Spitz, Margaret R., Wistuba, Ignacio I., Ozenberger, Bradley, Good, Peter J., Chang, Andrew C., Beer, David G., Watson, Mark A., Ladanyi, Marc, Broderick, Stephen, Yoshizawa, Akihiko, Travis, William D., Pao, William, Province, Michael A., Weinstock, George M., Varmus, Harold E., Gabriel, Stacey B., Lander, Eric S., Gibbs, Richard A., Meyerson, Matthew, Wilson, Richard K.

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Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes Autor Hindy, George, Dornbos, Peter, Chaffin, Mark D., Liu, Dajiang J., Wang, Minxian, Selvaraj, Margaret Sunitha, Zhang, David, Park, Joseph, Aguilar-Salinas, Carlos A., Antonacci-Fulton, Lucinda, Ardissino, Diego, Arnett, Donna K., Aslibekyan, Stella, Atzmon, Gil, Ballantyne, Christie M., Barajas-Olmos, Francisco, Barzilai, Nir, Becker, Lewis C., Bielak, Lawrence F., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bonnycastle, Lori L., Bottinger, Erwin, Bowden, Donald W., Bown, Matthew J., Brody, Jennifer A., Broome, Jai G., Burtt, Noël P., Cade, Brian E., Centeno-Cruz, Federico, Chan, Edmund, Chang, Yi-Cheng, Chen, Yii-Der I., Cheng, Ching-Yu, Choi, Won Jung, Chowdhury, Rajiv, Contreras-Cubas, Cecilia, Córdova, Emilio J., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Danesh, John, de Vries, Paul S., DeFronzo, Ralph A., Doddapaneni, Harsha, Duggirala, Ravindranath, Dutcher, Susan K., Ellinor, Patrick T., Emery, Leslie S., Florez, Jose C., Fornage, Myriam, Freedman, Barry I., Fuster, Valentin, Garay-Sevilla, Ma. Eugenia, García-Ortiz, Humberto, Germer, Soren, Gibbs, Richard A., Gieger, Christian, Glaser, Benjamin, Gonzalez, Clicerio, Gonzalez-Villalpando, Maria Elena, Graff, Mariaelisa, Graham, Sarah E., Grarup, Niels, Groop, Leif C., Guo, Xiuqing, Gupta, Namrata, Han, Sohee, Hanis, Craig L., Hansen, Torben, He, Jiang, Heard-Costa, Nancy L., Hung, Yi-Jen, Hwang, Mi Yeong, Irvin, Marguerite R., Islas-Andrade, Sergio, Jarvik, Gail P., Kang, Hyun Min, Kardia, Sharon L.R., Kelly, Tanika, Kenny, Eimear E., Khan, Alyna T., Kim, Bong-Jo, Kim, Ryan W., Kim, Young Jin, Koistinen, Heikki A., Kooperberg, Charles, Kuusisto, Johanna, Kwak, Soo Heon, Laakso, Markku, Lange, Leslie A., Lee, Jiwon, Lee, Juyoung, Lee, Seonwook, Lehman, Donna M., Lemaitre, Rozenn N., Linneberg, Allan, Liu, Jianjun, Loos, Ruth J.F., Lubitz, Steven A., Lyssenko, Valeriya, Ma, Ronald C.W., Martin, Lisa Warsinger, Martínez-Hernández, Angélica, Mathias, Rasika A., McGarvey, Stephen T., McPherson, Ruth, Meigs, James B., Meitinger, Thomas, Melander, Olle, Mendoza-Caamal, Elvia, Metcalf, Ginger A., Mi, Xuenan, Mohlke, Karen L., Montasser, May E., Moon, Jee-Young, Moreno-Macías, Hortensia, Morrison, Alanna C., Muzny, Donna M., Nelson, Sarah C., Nilsson, Peter M., O’Connell, Jeffrey R., Orho-Melander, Marju, Orozco, Lorena, Palmer, Colin N.A., Palmer, Nicholette D., Park, Cheol Joo, Park, Kyong Soo, Pedersen, Oluf, Peralta, Juan M., Peyser, Patricia A., Post, Wendy S., Preuss, Michael, Psaty, Bruce M., Qi, Qibin, Rao, D.C., Redline, Susan, Reiner, Alexander P., Revilla-Monsalve, Cristina, Rich, Stephen S., Samani, Nilesh, Schunkert, Heribert, Schurmann, Claudia, Seo, Daekwan, Seo, Jeong-Sun, Sim, Xueling, Sladek, Rob, Small, Kerrin S., So, Wing Yee, Stilp, Adrienne M., Tai, E. Shyong, Tam, Claudia H.T., Taylor, Kent D., Teo, Yik Ying, Thameem, Farook, Tomlinson, Brian, Tsai, Michael Y., Tuomi, Tiinamaija, Tuomilehto, Jaakko, Tusié-Luna, Teresa, Udler, Miriam S., van Dam, Rob M., Vasan, Ramachandran S., Viaud Martinez, Karine A., Wang, Fei Fei, Wang, Xuzhi, Watkins, Hugh, Weeks, Daniel E., Wilson, James G., Witte, Daniel R., Wong, Tien-Yin, Yanek, Lisa R., Kathiresan, Sekar, Rader, Daniel J., Rotter, Jerome I., Boehnke, Michael, McCarthy, Mark I., Willer, Cristen J., Natarajan, Pradeep, Flannick, Jason A., Khera, Amit V., Peloso, Gina M.

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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility Autor Wessel, Jennifer, Chu, Audrey Y, Willems, Sara M, Wang, Shuai, Yaghootkar, Hanieh, Brody, Jennifer A, Dauriz, Marco, Hivert, Marie-France, Raghavan, Sridharan, Lipovich, Leonard, Hidalgo, Bertha, Fox, Keolu, Huffman, Jennifer E, An, Ping, Lu, Yingchang, Rasmussen-Torvik, Laura J, Grarup, Niels, Ehm, Margaret G, Li, Li, Baldridge, Abigail S, Stančáková, Alena, Abrol, Ravinder, Besse, Céline, Boland, Anne, Bork-Jensen, Jette, Fornage, Myriam, Freitag, Daniel F, Garcia, Melissa E, Guo, Xiuqing, Hara, Kazuo, Isaacs, Aaron, Jakobsdottir, Johanna, Lange, Leslie A, Layton, Jill C, Li, Man, Hua Zhao, Jing, Meidtner, Karina, Morrison, Alanna C, Nalls, Mike A, Peters, Marjolein J, Sabater-Lleal, Maria, Schurmann, Claudia, Silveira, Angela, Smith, Albert V, Southam, Lorraine, Stoiber, Marcus H, Strawbridge, Rona J, Taylor, Kent D, Varga, Tibor V, Allin, Kristine H, Amin, Najaf, Aponte, Jennifer L, Aung, Tin, Barbieri, Caterina, Bihlmeyer, Nathan A, Boehnke, Michael, Bombieri, Cristina, Bowden, Donald W, Burns, Sean M, Chen, Yuning, Chen, Yii-DerI, Cheng, Ching-Yu, Correa, Adolfo, Czajkowski, Jacek, Dehghan, Abbas, Ehret, Georg B, Eiriksdottir, Gudny, Escher, Stefan A, Farmaki, Aliki-Eleni, Frånberg, Mattias, Gambaro, Giovanni, Giulianini, Franco, Goddard, William A, Goel, Anuj, Gottesman, Omri, Grove, Megan L, Gustafsson, Stefan, Hai, Yang, Hallmans, Göran, Heo, Jiyoung, Hoffmann, Per, Ikram, Mohammad K, Jensen, Richard A, Jørgensen, Marit E, Jørgensen, Torben, Karaleftheri, Maria, Khor, Chiea C, Kirkpatrick, Andrea, Kraja, Aldi T, Kuusisto, Johanna, Lange, Ethan M, Lee, I T, Lee, Wen-Jane, Leong, Aaron, Liao, Jiemin, Liu, Chunyu, Liu, Yongmei, Lindgren, Cecilia M, Linneberg, Allan, Malerba, Giovanni, Mamakou, Vasiliki, Marouli, Eirini, Maruthur, Nisa M, Matchan, Angela, McKean-Cowdin, Roberta, McLeod, Olga, Metcalf, Ginger A, Mohlke, Karen L, Muzny, Donna M, Ntalla, Ioanna, Palmer, Nicholette D, Pasko, Dorota, Peter, Andreas, Rayner, Nigel W, Renström, Frida, Rice, Ken, Sala, Cinzia F, Sennblad, Bengt, Serafetinidis, Ioannis, Smith, Jennifer A, Soranzo, Nicole, Speliotes, Elizabeth K, Stahl, Eli A, Stirrups, Kathleen, Tentolouris, Nikos, Thanopoulou, Anastasia, Torres, Mina, Traglia, Michela, Tsafantakis, Emmanouil, Javad, Sundas, Yanek, Lisa R, Zengini, Eleni, Becker, Diane M, Bis, Joshua C, Brown, James B, Adrienne Cupples, L, Hansen, Torben, Ingelsson, Erik, Karter, Andrew J, Lorenzo, Carlos, Mathias, Rasika A, Norris, Jill M, Peloso, Gina M, Sheu, Wayne H.-H., Toniolo, Daniela, Vaidya, Dhananjay, Varma, Rohit, Wagenknecht, Lynne E, Boeing, Heiner, Bottinger, Erwin P, Dedoussis, George, Deloukas, Panos, Ferrannini, Ele, Franco, Oscar H, Franks, Paul W, Gibbs, Richard A, Gudnason, Vilmundur, Hamsten, Anders, Harris, Tamara B, Hattersley, Andrew T, Hayward, Caroline, Hofman, Albert, Jansson, Jan-Håkan, Langenberg, Claudia, Launer, Lenore J, Levy, Daniel, Oostra, Ben A, O'Donnell, Christopher J, O'Rahilly, Stephen, Padmanabhan, Sandosh, Pankow, James S, Polasek, Ozren, Province, Michael A, Rich, Stephen S, Ridker, Paul M, Rudan, Igor, Schulze, Matthias B, Smith, Blair H, Uitterlinden, André G, Walker, Mark, Watkins, Hugh, Wong, Tien Y, Zeggini, Eleftheria, Laakso, Markku, Borecki, Ingrid B, Chasman, Daniel I, Pedersen, Oluf, Psaty, Bruce M, Shyong Tai, E, van Duijn, Cornelia M, Wareham, Nicholas J, Waterworth, Dawn M, Boerwinkle, Eric, Linda Kao, W H, Florez, Jose C, Loos, Ruth J.F., Wilson, James G, Frayling, Timothy M, Siscovick, David S, Dupuis, Josée, Rotter, Jerome I, Meigs, James B, Scott, Robert A, Goodarzi, Mark O

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